D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 53 Citations 10,020 174 World Ranking 11563 National Ranking 909

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • DNA
  • Mutation

His primary areas of investigation include Genetics, Mutation, Molecular biology, Gene and Pathology. He integrates many fields, such as Genetics and MICROCEPHALIN, in his works. The concepts of his Molecular biology study are interwoven with issues in Vimentin, Apoptosis, Macrophage migration inhibitory factor and Adenomatous polyposis coli.

His Adenomatous polyposis coli study integrates concerns from other disciplines, such as Stromal cell, Angiogenesis, Intestinal mucosa, Cytokine and Colorectal adenoma. In the subject of general Gene, his work in Familial exudative vitreoretinopathy, Genetic screen and Stop codon is often linked to TSPAN12 and FZD4, thereby combining diverse domains of study. His work deals with themes such as Carcinogenesis, Internal medicine and Immunofluorescence, which intersect with Pathology.

His most cited work include:

  • ASPM is a major determinant of cerebral cortical size. (447 citations)
  • Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain (344 citations)
  • Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13) (233 citations)

What are the main themes of his work throughout his whole career to date?

Alexander F. Markham mostly deals with Genetics, Gene, Molecular biology, Locus and Mutation. His study in Gene mapping, Exon, Genome, Sequence analysis and DNA sequencing falls within the category of Genetics. His biological study spans a wide range of topics, including Cancer research and Virology.

Alexander F. Markham has included themes like Biochemistry, DNA, DNA repair, Point mutation and Complementary DNA in his Molecular biology study. In most of his Locus studies, his work intersects topics such as Haplotype. His research on Mutation often connects related areas such as Internal medicine.

He most often published in these fields:

  • Genetics (50.26%)
  • Gene (25.13%)
  • Molecular biology (20.51%)

What were the highlights of his more recent work (between 2012-2021)?

  • Genetics (50.26%)
  • Nanotechnology (5.13%)
  • Computational biology (8.21%)

In recent papers he was focusing on the following fields of study:

His scientific interests lie mostly in Genetics, Nanotechnology, Computational biology, In vivo and Exome sequencing. He connects Genetics with TSPAN12 in his study. His work on Surface plasmon resonance and Nanomaterials as part of his general Nanotechnology study is frequently connected to Fabrication and Particle, thereby bridging the divide between different branches of science.

His study on Computational biology also encompasses disciplines like

  • DNA sequencing and related Gene duplication,
  • Data mining, which have a strong connection to Ontology, Candidate gene and Genetic linkage. As a member of one scientific family, Alexander F. Markham mostly works in the field of In vivo, focusing on Cancer research and, on occasion, Adenoma, Mdm2, Bioinformatics, Gene and Biomarker. Alexander F. Markham combines subjects such as Neurodevelopmental disorder, Genome, Nonsense mutation and Compound heterozygosity with his study of Exome sequencing.

Between 2012 and 2021, his most popular works were:

  • Engineering Gold Nanotubes with Controlled Length and Near‐Infrared Absorption for Theranostic Applications (53 citations)
  • HEATR2 Plays a Conserved Role in Assembly of the Ciliary Motile Apparatus (42 citations)
  • Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy (39 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • DNA
  • Mutation

Alexander F. Markham spends much of his time researching Genetics, Nanotechnology, Exome sequencing, Preclinical imaging and Fabrication. His study deals with a combination of Genetics and Ciliary Motility Disorders. His Nanotechnology research incorporates elements of Crystallinity and Biodistribution.

His studies in Exome sequencing integrate themes in fields like Molecular genetics, Consanguinity, Ubiquitin ligase and Massive parallel sequencing. His Nanomaterials research integrates issues from Nanofiber, One-Step, Bifunctional and Nanostructure. His Exome study combines topics from a wide range of disciplines, such as Disease gene identification, Genome, Genotyping, Genotype and Sequence analysis.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

ASPM is a major determinant of cerebral cortical size.

Jacquelyn Bond;Emma Roberts;Ganesh H. Mochida;Ganesh H. Mochida;Daniel J. Hampshire.
Nature Genetics (2002)

692 Citations

Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain

Andrew P. Jackson;Andrew P. Jackson;Helen Eastwood;Sandra M. Bell;Jimi Adu.
American Journal of Human Genetics (2002)

511 Citations

EB1, a protein which interacts with the APC tumour suppressor, is associated with the microtubule cytoskeleton throughout the cell cycle.

E E Morrison;B N Wardleworth;J M Askham;A F Markham.
Oncogene (1998)

326 Citations

Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)

Arthur B. McKie;John C. McHale;T. Jeffrey Keen;Emma E. Tarttelin.
Human Molecular Genetics (2001)

318 Citations

Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy

Sandeep Uppal;Sandeep Uppal;Christine P Diggle;Ian M Carr;Colin W G Fishwick.
Nature Genetics (2008)

293 Citations

Localization of cyclooxygenase-2 in human sporadic colorectal adenomas.

Keith S. Chapple;Elizabeth J. Cartwright;Gillian Hawcroft;Alison Tisbury.
American Journal of Pathology (2000)

267 Citations

Reduced expression of oestrogen receptor beta in invasive breast cancer and its re-expression using DNA methyl transferase inhibitors in a cell line model.

George P Skliris;Kailas Munot;Kailas Munot;Sandra M Bell;Pauline J Carder.
The Journal of Pathology (2003)

260 Citations

Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy.

Carmel Toomes;Nicola J. Marchbank;David A. Mackey;Jamie E. Craig.
Human Molecular Genetics (2001)

211 Citations

Dysregulated lymphocyte proliferation and differentiation in patients with rheumatoid arthritis

Frederique Ponchel;Ann W. Morgan;Sarah J. Bingham;Mark Quinn.
Blood (2002)

208 Citations

Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

James A. Poulter;Manir Ali;David F. Gilmour;Aine Rice.
American Journal of Human Genetics (2010)

204 Citations

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